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Triphenylen-1-ol, with the chemical formula C18H14O, is a colorless solid at room temperature. It is insoluble in water but readily soluble in organic solvents. triphenylen-1-ol is known for its unique structure and reactivity, making it a valuable building block in organic synthesis for the creation of more complex molecules. Additionally, it has potential applications in materials science, where it can be integrated into polymers and other materials to bestow particular characteristics. However, due to limited available information on its specific uses and potential hazards, further research is necessary to fully comprehend its properties and applications.

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  • 76885-34-2 Structure
  • Basic information

    1. Product Name: triphenylen-1-ol
    2. Synonyms: 1-Triphenylenol
    3. CAS NO:76885-34-2
    4. Molecular Formula: C18H12O
    5. Molecular Weight: 244.2873
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76885-34-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 498.2°C at 760 mmHg
    3. Flash Point: 240.4°C
    4. Appearance: N/A
    5. Density: 1.284g/cm3
    6. Vapor Pressure: 1.5E-10mmHg at 25°C
    7. Refractive Index: 1.804
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: triphenylen-1-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: triphenylen-1-ol(76885-34-2)
    12. EPA Substance Registry System: triphenylen-1-ol(76885-34-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 76885-34-2(Hazardous Substances Data)

76885-34-2 Usage

Uses

Used in Organic Synthesis:
Triphenylen-1-ol is utilized as a building block in organic synthesis for the creation of more complex molecules, leveraging its distinctive structure and reactivity.
Used in Materials Science:
In the field of materials science, triphenylen-1-ol is used for incorporating into polymers and other materials to impart specific properties, capitalizing on its potential to enhance material characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 76885-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76885-34:
(7*7)+(6*6)+(5*8)+(4*8)+(3*5)+(2*3)+(1*4)=182
182 % 10 = 2
So 76885-34-2 is a valid CAS Registry Number.

76885-34-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenylen-1-ol

1.2 Other means of identification

Product number -
Other names 1-Triphenylenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76885-34-2 SDS

76885-34-2Downstream Products

76885-34-2Relevant articles and documents

Atomic Force Microscopy Identifying Fuel Pyrolysis Products and Directing the Synthesis of Analytical Standards

Fatayer, Shadi,Poddar, Nimesh B.,Quiroga, Sabela,Schulz, Fabian,Schuler, Bruno,Kalpathy, Subramanian V.,Meyer, Gerhard,Pérez, Dolores,Guitián, Enrique,Pe?a, Diego,Wornat, Mary J.,Gross, Leo

, p. 8156 - 8161 (2018)

Here we present a new method that integrates atomic force microscopy (AFM) with analytical tools such as high-performance liquid chromatography (HPLC) with diode-array ultraviolet-visible (UV) absorbance, and mass spectrometry (MS) along with synthetic ch

Organic electroluminescent materials and devices

-

Page/Page column 77, (2018/06/26)

The present disclosure provides novel compounds containing dibenzo[fg,op]tetracene and larger all-benzenoid moiety that can be used as hosts for phosphorescent emitters providing low-voltage, high-efficiency and high-stability devices.

Water-promoted synthesis of fused bicyclic triazolines and naphthols from oxa(aza)bicyclic alkenes and transformation: Via a novel ring-opening/rearrangement reaction

Chen, Wenkun,Yang, Wen,Wu, Ruihua,Yang, Dingqiao

supporting information, p. 2512 - 2518 (2018/06/11)

An efficient three-component domino reaction among oxa(aza)bicyclic alkenes, sodium azide, and primary haloalkanes is reported, which offers a mild access to 1,2,3-triazolines in an aqueous medium with excellent diastereoselectivities and yields. Further studies show that, water-promoted isomerization of oxa(aza)bicyclic alkenes can afford 1-naphthol derivatives in good yields. Water not only promotes the reaction, but also provides a recyclable and sustainable approach to the desired product. In addition, a novel metal-free cascade ring-opening/rearrangement reaction of the obtained bicyclic triazolines to form multifunctionalized indenes has been discovered.

Isomerization of 7-oxabenzonorbornadienes into naphthols catalyzed by [RuCl2(CO)3]2

Ballantine, Melissa,Menard, Michelle L.,Tam, William

supporting information; experimental part, p. 7570 - 7573 (2009/12/28)

(Chemical Equation Presented) Ruthenium-catalyzed isomerization of 7-oxanorbornadienes into naphthols was investigated. Among the various ruthenium catalysts tested, [RuCl2(CO)3]2 gave the highest yields in the isomerizati

Palladium-catalyzed [2 + 2 + 2] cycloadditions of 3,4-didehydrophenanthrene and 1,2-didehydrotriphenylene

Romero, Carmen,Pena, Diego,Perez, Dolores,Guitian, Enrique

, p. 7996 - 8000 (2008/12/23)

(Chemical Equation Presented) Palladium-catalyzed [2 + 2 + 2] cycloaddition reactions of 3,4-didehydrophenanthrene (3,4-phenanthryne) and 1,2-didehydrotriphenylene (1,2-triphenylyne) afford sterically congested polycyclic aromatic hydrocarbons with novel

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